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NCT04401293 · ClinicalTrials.gov registry record · Phase 3

Full Dose Heparin Vs. Prophylactic Or Intermediate Dose Heparin in High Risk COVID-19 Patients

A Phase 3 study, sponsored by Northwell Health.

Completed
Registry status
Phase 3
Development phase
257
Enrollment target

NCT04401293: Completed Phase 3 study, sponsored by Northwell Health.

NCT04401293 is a Phase 3 study that has completed, run by Northwell Health. The registered enrollment target is 257 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04401293, a Phase 3 study, has completed, sponsored by Northwell Health.

COMPLETED
Registry status
Phase 3
Development phase
257 participants
Enrollment target

Study Summary

The aim of this study is to test the hypothesis that prophylaxis of severe COVID-19 patients with treatment dose LMWH leads to better thromboembolic-free outcomes and associated complications during hospitalization than prophylaxis with institutional standard of care with prophylactic to intermediate-doses of UFH or LMWH

Primary Outcome

Risk of arterial thromboembolic events (including myocardial infarction, stroke, systemic embolism), venous thromboembolism (including symptomatic deep vein thrombosis (DVT) of the upper or lower extremity, asymptomatic proximal DVT of the lower extremity, non-fatal pulmonary embolism (PE)), and all-cause mortality at Day 30 ± 2 days.

Interventions

  • DRUG Enoxaparin
  • DRUG Prophylactic/Intermediate Dose Enoxaparin

Trial Details

FieldValue
Enrollment Target 257 participants
Start Date 2020-04-26
Est. Completion 2021-05-14
Phase Phase 3
Northwell Health

370 total trials

What the finished NCT04401293 record still lists

NCT04401293 is an interventional study that assigns participants to a tested intervention. The registered 257 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 2 interventions - of which Enoxaparin is the first listed.

NCT04401293 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04401293 about?

NCT04401293 is a clinical study titled "Full Dose Heparin Vs. Prophylactic Or Intermediate Dose Heparin in High Risk COVID-19 Patients". The aim of this study is to test the hypothesis that prophylaxis of severe COVID-19 patients with treatment dose LMWH leads to better thromboembolic-free outcomes and associated complications during hospitalization than prophylaxis with institutional standard of care with prophylactic to intermediat...

What is the current status of trial NCT04401293?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 257 participants. The study started on 2020-04-26. Estimated completion is 2021-05-14.

What interventions are being tested in trial NCT04401293?

The interventions under investigation include: Enoxaparin (DRUG), Prophylactic/Intermediate Dose Enoxaparin (DRUG).

Who is sponsoring clinical trial NCT04401293?

This trial is sponsored by Northwell Health, which has 370 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04401293's enrollment target sits among peer trials

257 1238th of 2000 higher than 761 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04401293, the US trial registry maintained by the National Library of Medicine. NCT04401293 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.